D-850-2013 Class III Terminated
FDA drug recall D-850-2013 was initiated by GlaxoSmithKline, LLC. on Jul 18, 2013 and is designated Class III. Reason for recall: Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may contain EX TUMS Assorted Berries 750mg tablets The recall status is terminated (terminated May 18, 2016). Affected quantity: 300,480 bottles.
Recall details
- Product Type
- Drugs
- Report Date
- Aug 14, 2013
- Initiation Date
- Jul 18, 2013
- Termination Date
- May 18, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 300,480 bottles
Product description
TUMS, Antacid/Calcium Supplement, ULTRA Strength 1000, Assorted Berries, 72 Chewable Tablets, GlaxoSmithKline, Moon Twp, PA 15108, NDC 0135-0181-02
Reason for recall
Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may contain EX TUMS Assorted Berries 750mg tablets
Distribution pattern
U.S. Nationwide
Code information
Lot 3C11 and 3C11A
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-850-2013
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026